Burnett School of Biomedical Sciences, University of Central Floridagrid.170430.1, Orlando, Florida, USA.
mBio. 2022 Jun 28;13(3):e0031122. doi: 10.1128/mbio.00311-22. Epub 2022 Apr 25.
Population genomic analysis is a powerful tool to understand the evolutionary history of pathogens and the factors contributing to the success or failure of lineages. These studies have significant implications for human health, as evident from our ongoing tracking of SARS-CoV-2. In their article, Gill et al. (J. L. Gill, J. Hedge, D. J. Wilson, and R. C. MacLean, mBio 12:e02168-21, 2021, https://doi.org/10.1128/mBio.02168-21) demonstrate the utility of pathogen genomic data by comprehensively elucidating the origin of methicillin-resistant Staphylococcus aureus ST239. To accomplish this, they leveraged newly developed tools for querying large genomic data sets. Overall, these analyses rely on the availability of representative genomic data along with their associated metadata-information about where and when samples were collected, clinical and epidemiological characteristics, and phenotypic properties. However, in many instances, these data are missing. Here, I borrow the term "meaningful use" from the Health IT field to describe the need to maximize the utility of genomic data and make suggestions for how to address the current limitations.
人群基因组分析是一种强大的工具,可用于了解病原体的进化历史以及导致谱系成功或失败的因素。这些研究对人类健康具有重要意义,正如我们目前对 SARS-CoV-2 的跟踪所表明的那样。在他们的文章中,Gill 等人(J. L. Gill、J. Hedge、D. J. Wilson 和 R. C. MacLean,mBio 12:e02168-21,2021,https://doi.org/10.1128/mBio.02168-21)通过全面阐明耐甲氧西林金黄色葡萄球菌 ST239 的起源,展示了病原体基因组数据的实用性。为了实现这一目标,他们利用了新开发的工具来查询大型基因组数据集。总的来说,这些分析依赖于代表性基因组数据及其相关元数据的可用性——有关样本采集的地点和时间、临床和流行病学特征以及表型特性的信息。然而,在许多情况下,这些数据是缺失的。在这里,我借用了医疗信息技术领域的“有意义使用”一词来描述最大限度地提高基因组数据实用性的必要性,并提出了如何解决当前局限性的建议。